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Article

[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome].

Acta medica portuguesa - 1 Jan 2000

Costa Elísio, Vieira Emilia, Cleto Esmeralda, Cabeda José M, Pinho Luciana, Coimbra Eduarda, Dos Santos Rosário, Barbot José

Abstract excerpt

The aim of this work was to evaluate the influence of abnormal UDP-glucoronosyltransferase-1 (UGT1A1) gene variant, on the incidence and severity of neonatal hyperbilirubinemia, in glucose-6-phosphate dehydrogenase (G6PD) deficient newborns. The A(TA)nTAA region in the promoter of the UGT1A1 gene...

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Share to Anemia, Hemolytic, Congenital Nonspherocytic
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PMID: 12680285

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-12680285-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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